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Journal of Clinical Microbiology, August 1998, p. 2301-2307, Vol. 36, No. 8
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Evaluation of PCR, Culture, and Serology for
Diagnosis of Chlamydia pneumoniae Respiratory
Infections
R. P.
Verkooyen,1,*
D.
Willemse,1
S. C. A. M.
Hiep-van Casteren,2
S. A.
Mousavi Joulandan,3
R. J.
Snijder,2
J.
M. M.
van den Bosch,2
H. P. T.
van
Helden,4
M. F.
Peeters,5 and
H.
A.
Verbrugh1
Department of Medical Microbiology and
Infectious Diseases, Erasmus University Medical Center Rotterdam,
Rotterdam,1
Departments of Pulmonary
Diseases2 and
Medical Microbiology and
Immunology,4 St. Antonius Hospital,
Nieuwegein,2
Department of Medical
Microbiology, Diakonessen Hospital,
Utrecht,3 and
Department of Medical
Microbiology, St. Elisabeth Hospital,
Tilburg,5 The Netherlands
Received 4 December 1997/Returned for modification 27 January
1998/Accepted 30 April 1998
We prospectively studied 156 patients with a diagnosis of
community-acquired pneumonia requiring admission. Several respiratory specimens were obtained for the detection of Chlamydia
pneumoniae by cell culture and PCR. Three serum samples were
obtained from each patient. Serological diagnosis of a C. pneumoniae infection was determined by the
microimmunofluorescence (MIF) test, the complement fixation (CF) test,
and recombinant lipopolysaccharide (LPS) enzyme-linked immunosorbent
assay (ELISA; referred to as the rDNA LPS ELISA). Twenty-three patients
(15%) had serological results compatible with acute C. pneumoniae infection; nine (39%) of these subjects were C. pneumoniae PCR positive. Twenty-two patients (14%) had positive
PCR results without serological evidence of an acute C. pneumoniae infection. An attempt was made to calculate the
sensitivities and specificities of the MIF test, rDNA LPS ELISA, and
PCR for the diagnosis of chlamydial community-acquired pneumonia.
Several "gold standards" were defined. Generally, the sensitivities
of the rDNA LPS ELISA and MIF were comparable, while the sensitivity of
the CF test was shown to be very low. Independent of the gold standard
used, the best PCR results were obtained with nasopharyngeal specimens.
However, the predictive value of a positive C. pneumoniae
PCR result for patients with community-acquired pneumonia remains
unknown and may be low. Although a widely accepted gold standard is
still lacking, the rDNA LPS ELISA may currently be the preferred tool
for diagnosing acute respiratory Chlamydia infections in
routine clinical practice. However, the MIF test remains the method of
choice for determining the prevalence of C. pneumoniae
infections in a given community.
*
Corresponding author. Mailing address: Department of
Medical Microbiology and Infectious Diseases, Erasmus University
Medical Center, Rotterdam, Room Ee1720, P.O. box 1738, 3000 DR
Rotterdam, The Netherlands. Phone: 31 10 463 3510. Fax: 31 10 463 4730. E-mail: Verkooyen{at}kmic.fgg.eur.nl.
Journal of Clinical Microbiology, August 1998, p. 2301-2307, Vol. 36, No. 8
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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